| NDC Code | 60687-312-01 |
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| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-312-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-312-11) |
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| Product NDC | 60687-312 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Bupropion Hydrochloride |
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| Non-Proprietary Name | Bupropion Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20170412 |
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| End Marketing Date | 20250331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077284 |
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| Manufacturer | American Health Packaging |
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| Substance Name | BUPROPION HYDROCHLORIDE |
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| Strength | 150 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA] |
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